The Effects of Unfiltered (Turkish) Coffee Consumption on Cardiovascular Risk Parameters

NCT ID: NCT03495336

Last Updated: 2018-04-12

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

28 participants

Study Classification

INTERVENTIONAL

Study Start Date

2017-03-22

Study Completion Date

2017-10-22

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

Purpose/Objective: The aim of this study is to investigate the impact of boiled unfiltered (Turkish) coffee consumption on the plasma cardiovascular risk parameters of healthy subjects. The study also explores whether two unfiltered boiled (Turkish) coffee beverages that differ in content due to different roasting degrees will differentially affect cardiovascular biomarkers.

Methods: In this crossover intervention study, healthy, nonsmoking, habitual Turkish coffee drinkers (n=28) were randomized to consume at least 3 cups of Light (LR) or Dark (DR) roast Turkish coffee brews per day for 4 weeks after a washout period (WO) of 2 weeks. Subsequent to each coffee abstinence period, both groups received the alternative intervention. After the first WO and the coffee intervention periods, anthropometric measures, blood pressure, heart rate and 13 biochemical parameters were collected and dietary records were completed.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Background: Considerable controversy exists regarding the link between coffee consumption and cardiovascular disease (CVD) risk. It has been shown that different coffee preparation and brewing methods influence the concentration of compounds present in the final coffee brew. Unlike coffee traditionally consumed in the western world, Turkish coffee is not drip filtered, but rather its method of preparation involves slowly boiling water that is mixed with thinly ground coffee beans. This style of preparation results in a greater amount of biologically active components (caffeine and diterpenes) remaining in the liquid. In addition to preparation styles, roasting process greatly affects the chemical composition of the coffee. Coffee types differing in content of major constituents differ with regard to cardiovascular health effects.

Purpose/Objective: The aim of this study is to investigate the impact of boiled unfiltered (Turkish) coffee consumption on the plasma cardiovascular risk parameters of healthy subjects. The study also explores whether two unfiltered boiled (Turkish) coffee beverages that differ in content due to different roasting degrees will differentially affect cardiovascular biomarkers.

Methods: In this crossover intervention study, healthy, nonsmoking, habitual Turkish coffee drinkers (n=28) were randomized to consume at least 3 cups of Light (LR) or Dark (DR) roast Turkish coffee brews per day for 4 weeks after a washout period (WO) of 2 weeks. Subsequent to each coffee abstinence period, both groups received the alternative intervention. After the first WO and the coffee intervention periods, anthropometric measures, blood pressure, heart rate and 13 biochemical parameters were collected and dietary records were completed.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Cardiovascular Diseases

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

OTHER

Blinding Strategy

NONE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Washout period

Coffee abstention phase for 2 weeks.

Group Type EXPERIMENTAL

coffee abstention phase

Intervention Type OTHER

no coffee consumption for 2 weeks

Light roast coffee (LR)

Participants will follow LR Coffee consumption procedure and consume at least 3 cups of Light (LR) roast Turkish coffee brews per day for 4 weeks after a washout period (WO) of 2 weeks.

Group Type EXPERIMENTAL

LR Coffee consumption

Intervention Type OTHER

for 4 weeks participants consumed only LR Turkish coffee

Second washout period

coffee abstention phase for 2 weeks

Group Type EXPERIMENTAL

coffee abstention phase

Intervention Type OTHER

no coffee consumption for 2 weeks

Dark roast coffee (DR)

Participants will follow DR Coffee consumption procedure and consume at least 3 cups of Dark (DR) roast Turkish coffee brews per day for 4 weeks after a washout period (WO) of 2 weeks.

Group Type EXPERIMENTAL

DR Coffee consumption

Intervention Type OTHER

for 4 weeks participants consumed only DR Turkish coffee

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

coffee abstention phase

no coffee consumption for 2 weeks

Intervention Type OTHER

LR Coffee consumption

for 4 weeks participants consumed only LR Turkish coffee

Intervention Type OTHER

DR Coffee consumption

for 4 weeks participants consumed only DR Turkish coffee

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Regular Turkish coffee consumer ≥ 1 cups/day
* Body mass index (BMI) 18.5-24.9 kg/m2 )
* Non-smoker or former smoker (more than a year)
* Willingness to abstain from coffee drinking
* Willingness to consume ≥ 3 cups/day of Turkish coffee

Exclusion Criteria

* Acute or chronic diseases
* Severe illness with in-patient treatment during last 3 months
* Use of regular medication or any supplements
* Weight reduction ˃2 kg/week during the last month
* Pregnancy or breastfeeding
* Regular strong physical activity with ≥1h/day
* High alcohol intake a weekly intake of ˃7 units for women and ˃14units for men
* Excess consumption of total fat ˃35% of daily calories
* Consumption of saturated fatty acid ˃10% of daily calories
* Cholesterol intake ˃300mg/day
Minimum Eligible Age

20 Years

Maximum Eligible Age

35 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Eastern Mediterranean University

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Fatma Hülyam Eren

Instructor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Tanju Besler, Prof.

Role: STUDY_CHAIR

Eastern Mediterranean University

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Eastern Mediterrenean University

Famagusta, , Cyprus

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Cyprus

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

EasternMedU

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

The Effect of White Tea in Healthy Human Subjects
NCT07344688 ACTIVE_NOT_RECRUITING NA
Interindividual Variation in Response to Green Coffee
NCT06204445 ACTIVE_NOT_RECRUITING NA